82589-47-7 Usage
Uses
Used in Pharmaceutical Synthesis:
2-(3-methoxybenzyl)pyrrolidine-1-carbaldehyde is used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. Its presence in the molecular structure of these compounds contributes to their therapeutic properties and effectiveness.
Used in Organic Chemistry Reactions:
2-(3-methoxybenzyl)pyrrolidine-1-carbaldehyde is used as a reagent in organic chemistry reactions, such as the synthesis of heterocyclic compounds. Its reactivity allows for the formation of complex molecular structures that are essential in the development of new chemical entities.
Used in Medicinal Chemistry and Drug Development:
2-(3-methoxybenzyl)pyrrolidine-1-carbaldehyde has potential applications in the field of medicinal chemistry and drug development. Its unique structural features and reactivity make it a promising candidate for the design and synthesis of new drugs with improved therapeutic profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 82589-47-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,5,8 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 82589-47:
(7*8)+(6*2)+(5*5)+(4*8)+(3*9)+(2*4)+(1*7)=167
167 % 10 = 7
So 82589-47-7 is a valid CAS Registry Number.
82589-47-7Relevant academic research and scientific papers
Synthesis of Hexahydropyrroloisoquinolines - Analogs of Phenanthroindolizidine Anticancer Alkaloids
Gaur, S. P.,Jain, Padam C.,Anand, Nitya
, p. 46 - 51 (2007/10/02)
A convenient preparative route has been developed for the synthesis of hexahydropyrroloisoquinolines involving condensation of an araldehyde with ethyl 4-nitrobutanoate followed by LAH reduction and subsequent cyclization with H2SO4 to 2-arylmethylpyrrolidines.The latter on formylation and Bischler-Napieralsky cyclization followed by NaBH4 reduction give the required pyrroloisoquinolines.Using this method, 8-methoxy-1,2,3,5,10,10a-hexahydropyrroloisoquinoline (IXa); 7,8-dimethoxy-1,2,3,5,10,10a-hexahydropyrroloisoquinoline (IXb); 7,9,10,11,11a,12-hexahydrobenzopyrroloisoquinoline (Xa); 3-methoxy-7,9,10,11,11a,12-hexahydrobenzopyrroloisoquinoline (Xb); 7,7a,8,9,10,12-hexahydrobenzopyrroloisoquinoline (XIa); 3-methoxy-7,7a,8,9,10,12-hexahydrobenzopyrroloisoquinoline (XIb) and 2,3-dimethoxy-7,7a,8,9,10,12-hexahydrobenzopyrroloisoquinoline (XIc) have been synthesized.None of these compounds has shown any noteworthy anticancer activity while few have exhibited interesting antihistaminic, β-blocking, hypertensive, antiinflammatory and antireserpine activities.
